Lonza Houston, Inc.

Form 483 issued December 10, 2020 · Houston, Texas

Inspection
Dec 3 – Dec 10, 2020
Observations
4
Pages
5
FEI number
3013629214

In short: On December 10, 2020, FDA issued a Form 483 with 4 observations to Lonza Houston, Inc. in Houston, Texas (FEI 3013629214) after an inspection that ran Dec 3 – Dec 10, 2020. The investigators were Lauren M. Lilly, Scott Ballard and Steven E. Bowen. Most observations concern production and facilities & equipment; the most-cited regulation is 21 CFR 211.42 (design and construction features).

At a glance

Production and facilities & equipment account for 3 of 4 observations.

Production2
Facilities & equipment1
Materials1

What FDA observed

Preview: the opening words of each observation

Dashed: section inferred by FDA Intel and checked against the regulation text

  1. 01

    Physical and electronic control of material storage…

  2. 02

    The identity of each incoming batch of certain raw…

  3. 03

    Written procedures are not…

  4. 04

    Microbial contamination controls are…

The full 483

Plus the full detail behind each one, exactly as FDA wrote it.

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This inspection in context

Questions about this 483

What did FDA find at Lonza Houston, Inc.?

FDA listed 4 observations on this Form 483, mostly about production, facilities & equipment and materials. The most-cited regulation is 21 CFR 211.42 (design and construction features). The opening words of each observation are shown on this page.

Who inspected Lonza Houston, Inc.?

Lauren M. Lilly, Scott Ballard and Steven E. Bowen are named on this Form 483, for the inspection of Dec 3 – Dec 10, 2020. Each investigator has a profile showing what they cite most.

When was Lonza Houston, Inc. inspected by FDA?

The inspection ran Dec 3 – Dec 10, 2020, and the Form 483 is dated December 10, 2020.

How do I get the full Form 483 for Lonza Houston, Inc.?

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